Variant #0000167085 (NC_000001.10:g.171073038T>C, NM_001002294.2:c.245T>C (FMO3))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.171073038T>C
DNA change (hg38) g.171103897T>C
Published as -
ISCN -
DB-ID FMO3_000019 See all 3 reported entries
Variant remarks expected to influence metabolism of drug (xenobiotic) substrates of FMO3 that undergo N- or S- oxygenation
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0001 View details
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Date created 2013-03-01 17:32:06 +01:00 (CET)
Date last edited 2017-04-05 15:13:37 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 +/+ 3 c.245T>C - r.(?) p.(Met82Thr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.